CN1683417A - Process for preparing high substituted degree hydroxyalkyl starch - Google Patents
Process for preparing high substituted degree hydroxyalkyl starch Download PDFInfo
- Publication number
- CN1683417A CN1683417A CN 200510033407 CN200510033407A CN1683417A CN 1683417 A CN1683417 A CN 1683417A CN 200510033407 CN200510033407 CN 200510033407 CN 200510033407 A CN200510033407 A CN 200510033407A CN 1683417 A CN1683417 A CN 1683417A
- Authority
- CN
- China
- Prior art keywords
- starch
- preparation
- alpha
- alkylating reagent
- reaction
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Landscapes
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
The present invention relates to the preparation process of high substitution degree starch, and is hydroxyalkyl starch as a kind of non-ionic starch ether is widely used in daily chemical product, cosmetics, thickener, building adhesive, etc. The preparation process of the present invention includes mixing alpha-starch with catalyst inside oxygen-free sealed reaction container, adding alkylation reagent with certain water content to soak for 20-40 hr to obtain hydroxyalkyl starch with substitution degree as high as 2-3. During the reaction, there are no need of heating and no expansion danger, being favorable to industrial pnd.
Description
Technical field
The present invention relates to the preparation method of starch hydroxyalkylation prepared in reaction high substituted degree hydroxyalkyl starch.It mainly is starch is produced the high substitution value starch ethers through the hydroxyalkylation reaction manufacturing technology.
Background technology
Hydroxyalkyl starch belongs to the nonionic starch ethers, has good water-solubility and stability of viscidity, is widely used in printing-ink, fibrous warps starching, food and medicine product thickening cakingagent, daily-use chemical industry and makeup thickening material and material of construction tamanori etc.In recent years, only U.S.'s annual production is more than 100,000 ton.
The method for making of hydroxyalkyl starch has wet method, dry method and solvent method etc.Wet processing is the most common, and starch adds salt and makes the particle swelling inhibitor under the water and milk state, under alkaline catalysts and alkylating reagent effect, makes product at 35 ℃-50 ℃ reaction 8h-24h.The shortcoming of wet method is the product purification difficult, long reaction time, substitution value low (DS<0.1); Dry method be starch contain under the small amount of moisture with solid alkali and alkylating reagent gas at 85 ℃, make under 0.3MPa pressure and the sealed state.Dry method is a gas-solid phase reaction, product substitution value height, the danger but alkylating reagent is easily blasted; Solvent method is with organic solvent such as methyl alcohol, ethanol, Virahol, benzene etc. starch to be disperseed, under alkaline catalysts with the alkylating reagent reaction, product substitution value height, but exist solvent expensive, inflammable, poisonous, reclaim shortcomings such as difficulty; Recently also be suspended in the organic solvent by the independent water solution system that adopts emulsifying agent, starch, water, alkali, alkylating reagent to form and react, product separates from reaction mixture with solid particulate form.This method mild condition, product is refining simple, and reaction efficiency>75%, DS are between 0.5-2.5, and shortcoming is the system instability, the processing requirement height.
Summary of the invention
At the deficiencies in the prior art and shortcoming, the invention provides a kind of preparation method of high substitution value starch.
This method is under the airtight condition of anaerobic, is raw material with the Alpha-starch, under basic catalyst or salt, amines catalyst effect, with moisture alkylating reagent effect, under 0~38 ℃, reacted 20~40 hours, making high substitution value DS is 2~3 hydroxyalkyl starchs.
Adopt pre-gelatinized starch (claiming a-starch again) to make raw material, under basic catalyst or salt, amines catalyst effect,, make high substituted degree hydroxyalkyl starch with the alkylating reagent reaction.Temperature of reaction is 0 ℃-38 ℃, need not heat during reaction, also need not stir and stumble, just in encloses container, alkylating reagent soaked a-starch for some time after, remove reagent and obtain product.Starch is pulvis in the reaction process, makes the product separate easily to help suitability for industrialized production.
Adopting a-starch to make reaction raw materials, is best with no crystallinity.Test method is that a-starch is soaked in the cold water, does not have the polarisation cross with polarized light microscope observing and occurs, and illustrates that the starch crystals degree is destroyed, is easy to chemical reagent and enters.The starch of pre-half steaming still is the polarisation cross, alkylating reagent is infiltrated be obstructed, and the products therefrom substitution value is low and inhomogeneous, influences quality product.Make the a-starch material and can use starch such as wheat, rice, jowar, corn, cassava, potato, make by roll extrusion farinaceous size under the high temperature.The a-starch granules of making alkylated reaction is the smaller the better, should be less than 150 mesh sieve holes (Chinese Industrial Standards (CIS) sieve), generally wanted 150-200 mesh sieve hole (Chinese Industrial Standards (CIS) sieve), and in addition, as the starch that food is used, heavy metal content will meet state-set standard.Produce the also available dextrin of high substituted degree hydroxyalkyl starch.Dextrin is a starch through the product of different methods degraded, the product that is produced not as a-starch with the hydroxyalkyl starch viscosity of dextrin production.
Make the hydroxyalkylation catalysts with alkali, commonly used have sodium hydroxide, potassium hydroxide, a yellow soda ash etc., and also available salt or amines catalyst are as vitriol, carboxylate salt, tertiary amine etc.The most frequently used with sodium hydroxide.During use it is worn into behind the 0.02-0.04mm powder and a-starch uniform mixing, with the alkylating reagent reaction, if addition amount of sodium hydroxide is few, speed of response is slow again, and the product substitution value is low, and therefore, the sodium hydroxide optimum amount is the 1%-2% of starch weight.
Alkylating reagent is used oxyethane, propylene oxide or butylene oxide ring always.The above two boiling points are respectively 13 ℃ and 35 ℃, explosive, and their explosive range is very wide, and the alkylating reagent volume all can set off an explosion between 36%-78% after the air mixed.Therefore, reaction must be carried out under the airtight condition of anaerobic, and used reactor is that stainless steel is all-sealed, and the band explosion-proof equipment vacuumizes earlier before the reaction, feeds nitrogen again residual air is thrown out, and just adds alkylating reagent and reacts.Need not heat during reaction, generally soak starch 24h and promptly get product.As producing the low degree of substitution product, the reaction times can be shortened.Therefore, real reaction product substitution value is from 0, between the 5-3.0 or substitution value between 0.1~3, regulate.In the reaction process, the starch final water content is 10%-15%.The having of water is beneficial to sodium hydroxide and is ionized into ion and plays the catalyzed reaction effect.In fact general starch itself has contained 5% the moisture of having an appointment, these water adsorption are among starch, do not ooze out, make and be swift in response, the adding of a part of water is by with after alkylating reagent mixes in addition, join together in Alpha-starch and the mixture of catalysts, wherein the add-on of water is 2~10% of an Alpha-starch amount, adds moisture more again, during interpolation, can not pour water among the starch into, in order to avoid cause the local gelatinization of starch and blot the water phenomenon, can only be with water with after alkylating reagent mixes, join in the starch and go at once, to keep the particle form of starch, be beneficial to product separation and purify, guarantee the product homogeneity.After reaction finished, the elimination alkylating reagent led to hot water in reacting kettle jacketing, residual reagent is steamed walk to obtain rough hydroxyalkyl starch.If be used for food uses, must be further with the 50%-90% washing with alcohol, take off ethanol, citric acid is regulated PH6.5-7.0, drying, pulverize, sieve purified product.
The method that is used for measuring substitution value of the present invention is as follows:
With the hydroxypropylated starch is example, and the principle of measuring the bright basic starch substitution value of hydroxyl is identical with the mensuration propylene glycol, and with 1, the 2-propylene glycol is done standardized solution in the mensuration.1,2-propylene glycol, the bright basic starch of hydroxyl can generate the enol form and the olefine aldehydr formula dehydration neutralized rearrangement mixture of propionic aldehyde in the vitriol oil, this mixture generates violet complex at vitriol oil medium and triketohydrindene hydrate, use spectrophotometric determination, survey its absorbancy at the 595nm place, with standard 1, the 2-propylene glycol relatively can be derived the bright basic content of hydroxyl.
Above-mentioned reaction has utilized the open structure and the alkylating reagent reaction of a-starch, and at room temperature carry out, avoided the explosive danger of alkylating reagent, also avoided this reagent that the side reaction of auto-polymerization easily takes place under high temperature, high pressure, also reduce the hydrolytic action of alkylating reagent, obtained high substituted degree hydroxyalkyl starch.Reaction process starch remains solid state powder, is easy to separating reaction reagent, is easy to refined product, can be fit to suitability for industrialized production.
The advantage of the method for the invention, be open structure and the alkylating reagent reaction that has utilized Alpha-starch, and reaction process need not heating, avoided the explosive danger of alkylating reagent, also avoided this reagent that the side reaction of auto-polymerization easily takes place under high temperature, high pressure, also reduce the hydrolytic action of alkylating reagent, obtained high substituted degree hydroxyalkyl starch; Reaction process starch remains solid state powder, is easy to separating reaction reagent, is easy to refined product, can be fit to suitability for industrialized production.
Embodiment
Embodiment 1
The method for making of high substitution value hydroxypropyl starch.In the stainless steel cauldron that has chuck and explosion-proof equipment, 50Kg wheat Alpha-starch with moisture 5% (general Alpha-starch moisture 5%) and 1Kg granularity join in the reactor after mixed for the 0.02mm sodium hydroxide powder, after closing the lid, vacuumized 20 minutes, logical again nitrogen 20 minutes, join in the reactor after then the propylene oxide 180Kg of weight percent and 4Kg water being mixed, soak 24h, need not stir and heat during immersion, elimination propylene oxide then, in reacting kettle jacketing, feed 80 ℃ of hot water again,, obtain the hydroxypropylated starch of substitution value 2.5~3.0 in order to steam remaining propylene oxide.Product again through 90% washing with alcohol, reclaim ethanol, citric acid mix neutralization, dry, pulverize, sieving obtains the purified hydroxypropylated starch.Under the constant situation of above-mentioned technology, shorten the reaction times, also can obtain the hydroxypropylated starch of low degree of substitution.Propylene oxide after the recovery can also be used for the next batch reaction.
Embodiment 2
The method for making of high substitution value hydroxyethylamyle.Conversion unit and processing compound and reaction conditions are with embodiment 1.Propylene oxide with among the oxyethane replacement embodiment 1 obtains hydroxyethylamyle, and substitution value is 2.5~3.
Claims (7)
1, a kind of preparation method of high substituted degree hydroxyalkyl starch, it is characterized in that under the airtight condition of anaerobic, with the Alpha-starch is raw material, under basic catalyst or salt, amines catalyst effect, with moisture alkylating reagent effect, reacted 20~40 hours down at 0~38 ℃, making high substitution value DS is 2~3 hydroxyalkyl starchs.
2, preparation method according to claim 1 is characterized in that wheat, Chinese sorghum, soybean, rice, corn, cassava or the yam starch of described Alpha-starch for handling through pre-gelatinization, is optimum with no crystalline; Also can be the dextrin with above-mentioned starch preparation, the granularity of Alpha-starch especially can be 150-200 order Chinese Industrial Standards (CIS) sieve sieve aperture granularity less than 150 order Chinese Industrial Standards (CIS)s sieve sieve aperture.
3, preparation method according to claim 1 is characterized in that being that described catalyzer is sodium hydroxide, potassium hydroxide, yellow soda ash, vitriol, carboxylate salt or tertiary amine, especially can be sodium hydroxide, and the particle diameter of its catalyzer is 0.02~0.04mm.
4,, it is characterized in that being that described catalyzer sodium hydroxide optimum amount is the 1%-2% of starch weight according to claim 1 or 3 described preparation methods.
5, preparation method according to claim 1, it is characterized in that described moisture alkylating reagent, the adding that is meant water in this method steps is that water is by after mixing with alkylating reagent is first, mix mutually with Alpha-starch and mixture of catalysts, the water add-on is 2~10% of an Alpha-starch weight again.
6, preparation method according to claim 1 is characterized in that described alkylating reagent is oxyethane, propylene oxide or butylene oxide ring.
7, preparation method according to claim 1 is characterized in that can realizing substitution value between 0.5-3.0 by controlling reaction time, especially can adjust between 0.1~3.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 200510033407 CN1271087C (en) | 2005-03-07 | 2005-03-07 | Process for preparing high substituted degree hydroxyalkyl starch |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 200510033407 CN1271087C (en) | 2005-03-07 | 2005-03-07 | Process for preparing high substituted degree hydroxyalkyl starch |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1683417A true CN1683417A (en) | 2005-10-19 |
CN1271087C CN1271087C (en) | 2006-08-23 |
Family
ID=35262938
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN 200510033407 Expired - Fee Related CN1271087C (en) | 2005-03-07 | 2005-03-07 | Process for preparing high substituted degree hydroxyalkyl starch |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1271087C (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100491401C (en) * | 2006-07-28 | 2009-05-27 | 湖北省农业科学院辐照加工研究所 | Process of preparing non-ionic starch by initiating irradiation |
CN101942032A (en) * | 2010-09-07 | 2011-01-12 | 中科院广州化学有限公司 | Method for preparing methyl starch |
CN102344498A (en) * | 2011-10-26 | 2012-02-08 | 邹平福海科技发展有限公司 | Special starch ether for mortar and production method thereof |
CN104799093A (en) * | 2015-04-28 | 2015-07-29 | 防城港市雅美好饲料有限公司 | Preparation method of pregelatinized starch for aquatic feed |
CN104814271A (en) * | 2015-04-28 | 2015-08-05 | 防城港市雅美好饲料有限公司 | Preparation method for manufacturing feed with pre-gelatinized starch |
CN107226869A (en) * | 2017-06-29 | 2017-10-03 | 华南理工大学 | A kind of method that soda acid collaboration pretreatment prepares high substituted degree hydroxyl butyl starch |
CN110229241B (en) * | 2019-06-21 | 2021-07-20 | 华南理工大学 | Method for preparing potato hydroxypropyl starch based on cold plasma |
CN115960271A (en) * | 2023-01-17 | 2023-04-14 | 齐鲁工业大学(山东省科学院) | High-substitution-degree hydroxypropyl starch and preparation method and application thereof |
-
2005
- 2005-03-07 CN CN 200510033407 patent/CN1271087C/en not_active Expired - Fee Related
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100491401C (en) * | 2006-07-28 | 2009-05-27 | 湖北省农业科学院辐照加工研究所 | Process of preparing non-ionic starch by initiating irradiation |
CN101942032A (en) * | 2010-09-07 | 2011-01-12 | 中科院广州化学有限公司 | Method for preparing methyl starch |
CN101942032B (en) * | 2010-09-07 | 2012-05-30 | 中科院广州化学有限公司 | Preparation method of methyl starch |
CN102344498A (en) * | 2011-10-26 | 2012-02-08 | 邹平福海科技发展有限公司 | Special starch ether for mortar and production method thereof |
CN102344498B (en) * | 2011-10-26 | 2013-07-17 | 邹平福海科技发展有限公司 | Special starch ether for mortar and production method thereof |
CN104799093A (en) * | 2015-04-28 | 2015-07-29 | 防城港市雅美好饲料有限公司 | Preparation method of pregelatinized starch for aquatic feed |
CN104814271A (en) * | 2015-04-28 | 2015-08-05 | 防城港市雅美好饲料有限公司 | Preparation method for manufacturing feed with pre-gelatinized starch |
CN107226869A (en) * | 2017-06-29 | 2017-10-03 | 华南理工大学 | A kind of method that soda acid collaboration pretreatment prepares high substituted degree hydroxyl butyl starch |
CN110229241B (en) * | 2019-06-21 | 2021-07-20 | 华南理工大学 | Method for preparing potato hydroxypropyl starch based on cold plasma |
CN115960271A (en) * | 2023-01-17 | 2023-04-14 | 齐鲁工业大学(山东省科学院) | High-substitution-degree hydroxypropyl starch and preparation method and application thereof |
CN115960271B (en) * | 2023-01-17 | 2024-04-05 | 齐鲁工业大学(山东省科学院) | High-substitution hydroxypropyl starch and preparation method and application thereof |
Also Published As
Publication number | Publication date |
---|---|
CN1271087C (en) | 2006-08-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1271087C (en) | Process for preparing high substituted degree hydroxyalkyl starch | |
CN102477100B (en) | Esterification-etherification dual-modified starch and solid phase preparation method thereof | |
CN110590966B (en) | Preparation method of modified starch ether for improving tile adhesive sliding property | |
US4451649A (en) | Process for the production of hydroxypropyl starch | |
CN101250230A (en) | Method for preparing hydroxyethyl cellulose | |
CN100455601C (en) | Modification method of cellulose ether product | |
CN101070351B (en) | Polysubstituted radical cellulose composite ether and its preparing method | |
US2599620A (en) | Carboxymethyl ethers | |
CN110590965A (en) | Preparation method of modified starch ether for improving opening time of tile glue | |
CN115850805A (en) | Multipurpose modified hydroxypropyl starch for building materials as well as preparation method and application thereof | |
CN103601210B (en) | Wilkinite one step alkali is fused into the method for zeolite | |
CN101704532A (en) | Preparation method of zinc borate | |
CN101863993B (en) | Preparation method of sodium carboxymethyl starch with high substitution degree | |
CN101357994B (en) | Carboxymethyl wood flour with high degree of substitution and preparation method thereof | |
US3347855A (en) | Acetone slurry process for the preparation of soluble carboxymethyl cellulose | |
CN107502227B (en) | A kind of non-ionic starch based adhesive and preparation method thereof | |
CN101492167B (en) | Method for producing sodalite pure phase with shale ash | |
CN101024706B (en) | Preparing method of composite catalytic solid-phase prepared hydroxypropyl starch | |
US2801241A (en) | Process for the production of starch ethers | |
CN109534712B (en) | Light yellow naphthalene water reducing agent and preparation method thereof | |
CN1511851A (en) | Process for preparing pre-dextrinized hydropropyl di-starch phosphoric ester | |
CN1876638A (en) | Process for preparing benzoguanamine | |
CN102276733A (en) | Method for preparing ethyl cellulose with high degree of substitution | |
CN106749712A (en) | A kind of method that semidry method prepares CMS | |
CN105481990A (en) | Method for preparing hydroxypropyl starch through green high-pressure method |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20060823 Termination date: 20150307 |
|
EXPY | Termination of patent right or utility model |